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HRID 1876396作成日:2026年10月26日

Dimethyl Sulfoxide → Ethyl 2-(4-fluoro-2-methylphenoxy)-2-methylpropanoate

https://huagongshe.com/reaction/1876396

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物Potassium CarbonateHCID 11430—
反応物Propanoic acid, 2-bromo-2-methyl-, ethyl esterHCID 11745—
反応物4-Fluoro-2-methylphenolHCID 136295—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物Ethyl 2-(4-fluoro-2-methylphenoxy)-2-methylpropanoateHCID 67405334—

反応手順

A solution of 4-fluoro-2-methylphenol (10 g, 79.28 mmol), ethyl 2-bromoisobutyrate (23.2 mL, 158.6 mmol), potassium carbonate (21.9 g, 158.6 mmol), and DMSO (80 mL) was stirred at room temperature for 72 hours. Water and ethyl acetate were added and the layers were separated. The aqueous phase was extracted with ethyl acetate (3×50 mL) and the combined organic layers were washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The crude compound was purified by flash column chromatography on silica gel with hexanes and EtOAc (20%) to afford ethyl 2-(4-fluoro-2-methylphenoxy)-2-methylpropanoate. To a solution of ethyl 2-(4-fluoro-2-methylphenoxy)-2-methylpropanoate (13.3 g, 55.44 mmol) in tetrahydrofuran (40 mL) and methanol (10 mL) was added NaOH (6.66 g, 166.32 mmol) in water (14 mL) and stirred overnight. The volatiles were removed in vacuo and acidified with concentrated HCl. The milky white solution was extracted with ethyl acetate, dried over sodium sulfate, filtered and concentrated in vacuo to give 2-(4-fluoro-2-methylphenoxy)-2-methylpropanoic acid (658) as a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08309600B2
出典データセットuspto-grants-2012_11
ORD IDord-6d6bb607b02143e09086c6f024ef9b8e
出典メモuspto-grants-2012_11